← FDA DEVICE PRODUCT CODES
FDA PRODUCT CODE · CLASS II
SDT — Intra-Pulmonary Percussive Vibration (Ipv) Devices
It is intended to mobilize mucus using vibration and/or pressure delivered through a mouthpiece into the airways.
DEVICE CLASS
Class II
REGULATION
21 CFR 868.5665
MEDICAL SPECIALTY
Anesthesiology
REVIEW PANEL
AN
— Implant— Life-sustaining— GMP-exempt— Third-party review eligible
1
510(K)/PMA CLEARANCES
510k: 1
0
RECALL ENTRIES
Recent clearances
K241091Inogen, Inc. · 510k2024-12-23
Related on SPEQ
Source: FDA device classification, 510(k)/PMA, and recall datasets (openFDA). Recall entries count distinct FDA recall numbers, so one recall event affecting several products appears as several entries. SPEQ is not affiliated with the FDA; this is a reference view of public FDA data.
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